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临床试验/EUCTR2019-004148-31-NL
EUCTR2019-004148-31-NL进行中(未招募)1 期

The PREDMETH trial: Effectiveness of methotrexate versus prednisone as first-line therapy for pulmonary sarcoidosis – A randomized controlled trial - PREDMETH trial

Erasmus Medisch Centrum Dept. of Pulmonology0 个研究点目标入组 132 人开始时间: 2019年11月15日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
132

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Diagnosis of sarcoidosis according to the ATS/ERS/WASOG criteria (7), in case of absent histology a diagnosis of sarcoidosis can also be established in a multidisciplinary team meeting in a sarcoidosis expert center based on a highly suggestive clinical and radiological picture (18, 19)
  • - Age =18 years
  • - A pulmonary indication for treatment and parenchymal involvement on X-ray or CT-scan conducted within three months before inclusion (determined by the treating physician and conform current guidelines).
  • - A forced vital capacity (FVC) of =90% of predicted, or a diffusion capacity of the lung for carbon monoxide (DLCO) =70% of predicted, or =5% FVC decline/=10% DLCO decline in the past year. For pulmonary functions tests GLI reference values are used.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 82
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 50

排除标准

  • - Any condition or circumstance that, in the opinion of the investigator, may make a subject unlikely or unable to complete the study or comply with study procedures.
  • - Previous immunosuppressive treatment for sarcoidosis
  • - Use of systemic immunosuppressive therapy within the preceding three months for another disease than sarcoidosis
  • - Pregnant, breastfeeding, or planning to become pregnant or breastfeed during the study treatment or within 90 days after the last dose in the randomized study phase. For males; planning to pro-create during the study or within 90 days after the last dose of the randomized study phase.
  • - Contra-indication for methotrexate or corticosteroids:
  • severely impaired renal function (creatinine clearance <30 ml/min)
  • impaired hepatic function (serum bilirubin-value >5 mg/dl or 85,5 micromole/l)
  • bone marrow insufficiency with severe leukopenia, thrombocytopenia, or anaemia
  • severe acute or chronic infections, such as tuberculosis, HIV, parasitic infections or other immunodeficiency syndromes
  • mouth, stomach or duodenal ulcers

研究者

发起方
Erasmus Medisch Centrum Dept. of Pulmonology

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